ChemInform Abstract: RADIATIONLESS TRANSITIONS IN ELECTRON DONOR-ACCEPTOR COMPLEXES: POSITION-DEPENDENT DEUTERIUM ISOTOPE EFFECTS ON S1 → S0 INTERNAL CONVERSION OF 1:1 AND 2:1 COMPLEXES OF METHYL-SUBSTITUTED BENZENES WITH TETRACYANOBENZENE

1983 ◽  
Vol 14 (3) ◽  
Author(s):  
B. T. LIM ◽  
S. OKAJIMA ◽  
A. K. CHANDRA ◽  
E. C. LIM
1979 ◽  
Vol 20 (31) ◽  
pp. 2919-2920 ◽  
Author(s):  
F.M. Martens ◽  
J.W. Verhoeven ◽  
Th.J. de Boer

1976 ◽  
Vol 54 (19) ◽  
pp. 2974-2980 ◽  
Author(s):  
J. Bryan Jones ◽  
Keith E. Taylor

The rates of H-transfer between various 1,4-dihydropyridines and pyridinium salts (including NADH and NAD+), and from 1,4-dihydropyridines to FMN, have been measured. The reactions are found to be sufficiently slow for H-transfer to be rate-determining to a significant extent when such Systems are applied for nicotinamide coenzyme recycling purposes. The rates of H-transfer parallel the magnitudes of the donor–acceptor redox potential differences (ΔE0′); ΔE0′ values may therefore be used as qualitative guides in formulating and selecting redox couples of NAD/H recycling value. On the basis of deuterium isotope effects, it is concluded that formation of a complex prior to H-transfer is not rate determining for 1,4-dihydropyridine–NAD+ reactions. This behavior is in contrast to that of other model alcohol dehydrogenase Systems.


2000 ◽  
Vol 2 (5) ◽  
pp. 981-991 ◽  
Author(s):  
Kengo Suzuki ◽  
Attila Demeter ◽  
Wolfgang Kühnle ◽  
Erich Tauer ◽  
Klaas A. Zachariasse ◽  
...  

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